Canonical Allele Identifier: PA915984141
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127644
ClinVar RCV Id: RCV000115528 RCV000212583 RCV000524406 RCV000986649 RCV000195415 RCV001353804 RCV003492474 RCV001719858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu62Val
CA021100
NM_001258281.1:c.184C>G